Method of decontaminating a chamber that has movable shelves

ABSTRACT

A method of decontaminating or sterilizing chamber systems including freeze dryers at low temperature and pressure levels by utilizing vaporized sterilant, preferably hydrogen peroxide, peracetic acid and mixtures thereof is disclosed.

FIELD OF THE INVENTION

The present invention relates to a method for decontaminating anevacuated chamber having movable shelves containing or comprised ofcomplex and irregularly shaped articles. More particularly, theinvention relates to a method of introducing a sterilant vapor into anevacuated chamber by utilizing the movable shelves within the chamber tocontrollably release the vapor. The sterilant vapor is left in thechamber for a sufficient period of time to produce the desired level ofdecontamination.

BACKGROUND OF THE INVENTION

Chambers are used in many industries including the food and drugindustries for many different purposes; freeze drying and sterilizationare two such purposes. Freeze dryers used in the pharmaceutical andother industries traditionally include a freeze dryer chamber, shelvesin the chamber for holding the product(s) to be freeze dried, acondenser with refrigerator coils, a vacuum system, and piping forconnecting the freeze dryer components. Generally, the freeze dryershelves are heated and cooled during the freeze drying cycle withheating and cooling means, such as a heat transfer fluid circulatingthrough the shelves and a heat exchanger.

Typically, the products to be freeze dried are in loosely cappedcontainers, which are then placed on the freeze dryer shelves. After thechamber door is closed, the shelves are cooled to about -40° C. tofreeze the product. Thermocouples, or other temperature probes, indicatewhen the product is frozen and at the correct temperature. The freezedryer chamber and condenser are then evacuated through a top, side orrear port on the condenser to a deep vacuum of about 200 microns of Hg(1 Torr=1000 micron of Hg=1 mm of Hg) while the condenser coils arecooled to around -40° C. As sublimation of moisture from the productoccurs, it cools the product further. The shelves are warmed to maintainthe frozen product at the desired temperature.

The vaporous moisture from the product escapes from the loosely cappedcontainers and is drawn in vapor form from the containers in the chamberto the condenser. In the condenser, the vapor condenses and then freezeson the condenser coils.

This process continues until the product is sufficiently freeze dried asdetermined by known means. The chamber is vented to atmosphericpressure, the containers are capped (if it is desired), the chamber dooris opened, and the freeze dried product removed.

Traditionally, the condenser is defrosted before the next freeze dryingcycle using water or steam. The water or steam may be flowed through thecondenser or it may be used to flood the condenser. The chamber istypically isolated from the condenser during this process by a largebutterfly or mushroom valve. The condenser is drained at the end of thedefrost. The chamber is typically Cleaned-In-Place (C.I.P.) eithermanually or automatically between each load to remove any debris fromthe previous load.

Decontamination and sterilization of the chambers is currentlyaccomplished using formaldehyde vapor, ethylene oxide gas, peraceticacid, liquid hydrogen peroxide, or steam. Each of these methods presentsserious disadvantages. For the purposes of this invention the termdecontamination means a 3 log (or greater) reduction in bioburden andsterilization means a 6 log (or greater) reduction in bioburden.

Methods using formaldehyde vapor and ethylene oxide gas typicallyoperate at pressures below 15 psig and at temperatures below 140° F.;however, the sterilizing agents are undesirable because they areconsidered carcinogenic and may be harmful to the operator. Residualremoval is also a problem. Ammonia is used to neutralize theformaldehyde gas, leaving a white powder distributed throughout thefreeze dryer which is difficult to remove without compromisingsterility.

Ethylene oxide vapors can be removed and catalyzed during a lengthyaeration (i.e. more than 8 hours); however, various air/ethylene oxidemixtures which are present during the decontamination/sterilizationprocess are explosive. Consequently, ethylene oxide is typically mixedwith Freon 12, an ozone depletor which must be recovered at greatexpense.

Peracetic acid and liquid hydrogen peroxide may also be sprayedmanually, or automatically, throughout the interior of freeze dryers.This method, though, is ineffective on inaccessible areas such as thecondenser and "dead legs" (dead-ended piping or lumens) in the freezedryer unit. Completely flooding the freeze dryer is also not effectivesince air pockets will prevent the liquid from penetrating into many ofthe same inaccessible areas.

Steam is emerging as the method of choice. Steam sterilization, however,is achieved at very high temperatures and pressures. As a result, thismethod requires that the freeze dryer chamber, condenser and associatedpiping be subjected to high temperature and pressure. The combined highpressure and temperature of steam sterilization (e.g., 250° F. and 15psig) when alternated with freeze drying while deeply evacuated (at -40°F. and at approximately 200 microns of Hg absolute) takes its toll onthe reliability of the freeze dryer system. Furthermore, existing freezedryers which do not meet the required temperature/pressure requirementscannot be retrofit for steam decontamination/sterilization.

There is a need for a method which can decontaminate or sterilizechambers, particularly freeze dryers, in an economical and simplemanner. There is a further need for a method for decontaminating orsterilizing chambers, particularly freeze dryers, that can be applied onexisting chambers and freeze dryers. There is also a need for a methodfor decontaminating or sterilizing chambers particularly freeze dryers,without using hazardous sterilants or chemicals having hazardousdecomposition products which are harmful to the environment.

SUMMARY OF INVENTION

It is therefore a main object of the present invention to provide amethod of effectively decontaminating, and preferably sterilizing,chambers, particularly freeze dryers, in a simple and economical manner,without using hazardous sterilants or chemicals having hazardousdecomposition products.

Additional objects and advantages of the invention will be set forth inpart in the description which follows, and in part will be obvious fromthe description, or may be learned by practice of the invention. Theobjects and advantages of the invention may be realized and obtained bymeans of instrumentalities and combinations particularly pointed out inthe appended claims.

To achieve these objects and in accordance with the purpose of theinvention, the present invention provides a method of decontaminating,preferably sterilizing, a chamber system, particularly freeze dryersystem, with sterilant vapor, preferably hydrogen peroxide or peraceticacid vapor, at the completion of the freeze drying cycle, wherein thefreeze dryer comprises a freeze dryer chamber containing at least twoshelves, one of which is movable, and a condenser, which are fluidlycoupled to each other. Actual decontamination/sterilization isaccomplished by placing a container or containers holding apredetermined amount of liquid sterilant between the shelves in thefreeze dryer chamber, lowering the shelves thereby sealing thecontainer(s), deeply evacuating the freeze dryer components, raising theshelves which allows the liquid sterilant to vaporize by exposing it tothe evacuated environment, and exposing the freeze dryer components tothe vapor for a predetermined period. This process is then repeateduntil a predetermined level of decontamination is achieved. An aerationfollows. consisting of alternating system evacuation and venting untilall residuals have been removed.

The method may also be applied on a freeze dryer chamber least twoshelves are vertically movable while maintaining position horizontally.

The method may also be combined with a container apparatus comprisingmultiple individual containers, wherein each container comprises acompression spring, plunger, sealing device and a stop which varies inlength for each container, thereby allowing multiple sterilizationpulses to occur on any one movable shelf.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

The present invention overcomes the disadvantages of currentsterilization methods by first placing a predetermined amount of liquidsterilant, preferably liquid hydrogen peroxide or peracetic acid, in oneor more containers. The containers are uniformly distributed on a lowershelf of the chamber having at least two shelves, wherein an upper shelfmay be moved vertically without altering its position horizontally. Theuniform distribution of containers prevents the shelf raise/lowermechanism from binding and/or being damaged and may improve vaporizationefficiency. Each container comprises a compression spring and sealingdevice which may be broken in order to expose the contents to thechamber environment. In determining the amount of sterilant liquid whichshould be placed inside the container, the combined chamber andcondenser volume and sterilant concentration are considered For example,a freeze dryer with a combined chamber and condenser volume of 100liters (3.53 ft.³) would accept 2.2 mg/liter of 35% by weight of H₂ O₂vapor at 25° C. without exceeding below the dew point of the vapor.Accordingly, the following calculation is performed.

    2.2 mg/liter×100 liters×0.001 gram/mg×100 g solution/35 g H.sub.2 O.sub.2 =0.628 g solution.

The dew point can be calculated for a given chamber temperature andhydrogen peroxide solution concentration by using methodology outlinedin U.S. Pat. No. 4,956,145, the disclosure from which is incorporated byreference herewith.

For functional, as well as safety reasons, not more than 1 or 2 grams ofsolution should be placed in one container. The mass of liquid hydrogenperoxide must be small compared to the mass of the container so that theevaporative cooling of the sterilant is offset by heat transfer from thecontainer thereby preventing freezing. The liquid, however, can bedivided among several containers that are, for example, located in thecenter and each of the four corners of the shelf.

A loosely fitted cap is placed on the liquid filled container. The upperchamber shelf is lowered in order to press down on the container capand, hence, seal the containers. The chamber, condenser and piping arethen evacuated and the vacuum valves closed isolating the freeze dryersystem from the vacuum system. Following evacuation the upper shelf israised until the seals on the containers have been broken, allowing theexposed hydrogen peroxide to evaporate in the deeply evacuatedenvironment. The system remains under a deep vacuum for a pre-determinedtime period, exposing the interior of the freeze dryer to the hydrogenperoxide vapor. The pressure rise corresponding to the vaporization ofthe solution is dependent on both temperature and concentration of thesolution. Sterilization of all or the interior of the freeze dryer,condenser and piping will likely be incomplete in dead legs when most ofthe hydrogen peroxide vapor from a single exposure has broken down intowater vapor and oxygen. Hence, the above mentioned steps are thenrepeated until a pre-determined level of decontamination orsterilization is achieved. After decontamination/sterilization has beenachieved, the system is aerated by alternating system evacuation andventing until all residuals have been removed.

In a first embodiment of the invention, the freeze dryer chamberincludes two shelves, upper and lower, the upper one of which ismovable. A container holding a predetermined amount of liquid sterilant,preferably hydrogen peroxide or peracetic acid, more preferably about30-35% by weight concentration of aqueous solution of hydrogen peroxide,is loosely capped and placed within the freeze dryer chamber at thecenter of the lower shelf. Four additional empty containers are placedin each of the four corners of the chamber, preventing the shelfraise/lower mechanism from binding and/or being damaged. Alternately,the liquid sterilant may be distributed among the containers therebyimproving vaporization efficiency. The upper shelf is then lowered untilit presses on the cap and seals the liquid filled container. Thechamber, condenser and piping are evacuated to below 1 Torr absolutepressure, and then the chamber, condenser and piping are isolated fromthe vacuum system. Thereafter, the upper shelf is raised until the capis no longer sealed but rests loosely on the container. Because of thepressure differential between the evacuated chamber and the containers,the sterilant then vaporizes upon exposure to the deeply evacuatedenvironment and the vapor escapes into the chamber under the gapsbetween the cap and its container. The system is maintained under astatic deep vacuum for a pre-determined time period (e.g. 30 minutes),hence exposing the interior of the freeze dryer to sterilant vapor andachieving the decontamination. Air is vented into the freeze dryer,raising the pressure to about 50 Torr or greater before the chamber isre-evacuated. Then, the entire process can be repeated a number of timesso that the desirable level of decontamination or sterilization isachieved. The aeration begins by admitting air into the freeze dryer,raising the pressure to about 100 Torr or greater following by are-evacuation to 10 Torr or below. This aeration process is thenrepeated until the desired level of sterilant residual within thechamber is achieved.

In a second embodiment of the invention, the freeze drier system iscomprised of a chamber containing at least 3 shelves (bottom, middle andupper), two of which are vertically movable while maintaining thehorizontal position stoppable in any vertical position. Containersselectively filled with liquid sterilant are uniformly positioned oneach of the bottom and middle shelves. The middle shelf is first loweredto seal loosely fitting caps on the containers on the bottom shelfThereafter the top shelf is lowered to seal the containers on the middleshelf. The above mentioned process is then carried out sequentially oneach shelf wherein the chamber is evacuated, and the upper shelf israised in order to break the seal on the liquid filled containers,allowing the sterilant to evaporate in the deeply evacuated environmentand distribute within the chamber. After a specified time period ofexposure to the sterilant vapor, air is vented into the freeze dryer andthe chamber and condenser are re-evacuated in order to initiate theprocess using the liquid filled container on the bottom shelf.

In another embodiment of the invention, the freeze dryer system iscomprised of a chamber containing 3 or more vertically movable shelveswhich are stoppable in any position while maintaining a horizontalposition. Containers selectively filled with liquid sterilant areuniformly positioned on each of the shelves. The shelves are all loweredto seal all of the containers. The above mentioned process is thencarried out on each shelf thereby exposing the chamber, condenser andpiping to a number of sterilant vapor pulses which is equal to thenumber of shelves in the chamber.

In another embodiment of the invention, a container apparatus isutilized such that multiple sterilize pulses can be accomplished with asingle movable shelf. The container apparatus is comprised of multipleindividual containers, each having a compression spring, a sealingdevice and a stop which is of differing lengths for each container.Additionally, the bottoms of the containers have raised dimplespermitting the area on the shelf below the container to be sterilizedalso. Liquid sterilant is placed in each of the individual containers.In using the method of the current invention is aforementioned above,when the upper shelf is raised to a predetermined first level, forexample, 3/8 inch, the seal on the first container is broken in thedeeply evacuated environment and evaporation of the liquid sterilantcontained therein occurs. After an appropriate time period thesterilization pulse is completed by admitting filtered, air the systemis then re-evacuated and the upper shelf is raised to a predeterminedsecond level, for example, an additional 3/8 inch until the seal of thesecond container is broken. The pulsing sterilization process is thenrepeated until the upper shelf has moved sufficiently far to break theseals on all of the container apparatii.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention can best be understood by reference to thedrawings, in which:

FIG. 1 is a schematic diagram of one embodiment of a system comprisingtwo chamber shelves for use in practicing the method of the presentinvention.

FIG. 2 is a schematic diagram of an alternative system comprising fourshelves for use in practicing the method of the present invention.

FIG. 3 is a schematic diagram of the container apparatus portion of analternative system for use in practicing the method of the presentinvention.

FIGS. 4 and 5 are schematic diagrams of another embodiment of thecontainer apparatus portion of the alternative system for use inpracticing the method of the present invention.

DETAILED DESCRIPTION OF THE DRAWINGS

FIG. 1

The invention will first be described in reference to FIG. 1, whichillustrates components of a system for practicing a preferred embodimentof the invention.

The system, as depicted in FIG. 1, includes an upper movable shelf 1,container 2, cap 3 which loosely fits onto the container, and lowershelf 4. A predetermined amount of liquid sterilant, preferably hydrogenperoxide or peracetic acid, is poured into container 2. The loosefitting cap 3 is then put in place. The cap is designed so as to avoidhorizontal sliding but does not act as a plug to cork the container'sopening. The capped container is placed in the center of lower shelf 4.Then the chamber door of the freeze dryer (not shown) is closed andupper shelf 1 is lowered until it presses down on cap 3 and seals shutcontainer 2.

The chamber, condenser and piping are evacuated to below 1 Torr absolutepressure, following which upper shelf 1 is raised until cap 3 is nolonger sealed on container 2. The sterilant then vaporizes in the deeplyevacuated environment and diffuses out of the container into the freezedryer. The system remains under a static deep vacuum for apre-determined time period, exposing the interior of the freeze dryer tohydrogen peroxide vapor.

FIG. 2

The system as depicted in FIG. 2 includes top shelf 19, lower shelf 13,and upper shelf 16, all of which are stoppable in any position. Bottomshelf 10, however, remains stationary throughout the decontaminationsterilization procedure. Container 11 is first filled with apredetermined amount of liquid hydrogen peroxide and placed in thecenter of shelf 10. Shelf 13 is lowered, sealing cap 12 on container 11.Container 14 is similarly filled with liquid sterilant, preferablyhydrogen peroxide or peracetic acid, and placed in the center of shelf13. Cap 15 is fitted onto container 14 and shelf 16 is lowered to sealcap 15 onto container 14. Container 17 is then filled with apredetermined amount of liquid sterilant and placed in the center ofshelf 16. Cap 18 is loosely fitted onto container 17 and sealed thereonwhen shelf 19 is lowered, pressing against cap 18 until container 17 issealed.

The chamber, condenser and piping are evacuated to below 1 Torrabsolute. Shelf 19 is then raised until cap 18 no longer seals shutcontainer 17. The sterilant contained in container 17 is thus exposed tothe deeply evacuated environment and hence, vaporizes. The systemremains under a static deep vacuum for a time period during which theinterior of the chamber is exposed to sterilant vapor. Air is thenvented into the freeze dryer, raising the pressure to above 50 Torr.

Following aeration, the system is re-evacuated to below 1 Torr. Shelf 16is then raised until cap 15 no longer seals shut container 14, exposingthe sterilant to the deeply evacuated environment and, hence, causingvaporization. The system remains under a static deep vacuum for aspecified time period, during which the interior of the chamber isexposed to sterilant vapor. Air is again vented into the freeze dryer,raising the pressure to above 50 Torr.

Finally, shelf 13 is raised in a similar manner and the above describedprocedure is conducted with respect to container 11.

FIG. 3

The system as depicted in FIG. 3 includes upper shelf 30, containers 40,41 and 42, stops 50, 51 and 52, compression springs 53, 54, 55, plungers56, 57 and 58, caps 60, 61 and 62, and seals 63, 64 and 65. Apredetermined amount of liquid hydrogen peroxide is poured intocontainers 40, 41 and 42 which are sitting on the bottom shelf (notshown).

As the upper shelf 30 is lowered it pushes plungers 56, 57 and 58 down.Compression springs 53, 54 and 55 in turn push caps 60, 61 and 62 whichcontain seals 63, 64 and 65 against containers 40, 41 and 42 producing avacuum seal.

The chamber condenser and piping are evacuated to 1 Torr or less. Thevacuum piping is closed off. Shelf 30 is raised 1/8" past the point whenstop 50 prevents compression spring 53 from extending. Cap 60 and seal63 are no longer compressed against container 40 by the force ofcompression spring 53. Sterilant 66 is now exposed to the deeplyevacuated interior of the chamber so it evaporates and expands to fillthe void within the chamber, condenser and piping. After an appropriatetime interval, the chamber is vented to 50 Torr (or above) with filteredair.

The chamber, condenser and piping are re-evacuated to Torr or below andthe vacuum piping closed off. Shelf 30 is further raised 1/8" past thepoint when stop 51 prevents compression spring 54 from extending. Cap 61and seal 64 are no longer compressed against container 41 by the forceof compression spring 54.

Liquid sterilant solution 67, now exposed to the deeply evacuated state,evaporates and fills the void within the chamber condenser and piping.After an appropriate time interval, the chamber is vented to 50 Torr (orabove) with filtered air.

The chamber, condenser and piping are re-evacuated to 1 Torr, or below,and the vacuum piping closed off. Shelf 30 is further raised 1/8" pastthe point when stop 52 prevents compression spring 55 from extending.Cap 62 and seal 65 are no longer compressed against container 42 by theforce of compression spring 55.

Liquid sterilant solution 68, now exposed to the deep evacuatedenvironment with the chamber, evaporates and expands to fill the voidwithin the chamber, condenser and piping. After an appropriate timeinterval, the chamber is vented to 50 Torr (or above) with filtered air.

Evacuations are alternated with filtered air admits until the chamber,condenser and piping are sufficiently aerated to lower the hydrogenperoxide residuals to the desired level.

FIGS. 4 and 5

An alternate embodiment of the system described in FIG. 3, is depictedin FIGS. 4 and 5 includes upper shelf 130 and lower shelf 131 whichcompress and seal the container assembly consisting of container 102,plunger 104, cap 103, spring 105, seal 106, spring 107, plunger stop110, pushrod 108 and sterilant solution 109.

A deep vacuum, typically at or below 1 Torr, is drawn in the freezedryer chamber (not shown) which contains shelves 130 and 131 as well asthe entire container assembly. As shelf 130 begins to move away fromshelf 131, compression spring 105 extends until plunger stop 110 restsagainst the bottom surface of cap 103.

Then, spring 107 pushes plunger 104, cap 103 spring 105, plunger stop110 and seal 106 against top shelf 130 as it continues to move away fromshelf 131. The vacuum within the freeze dryer chamber is sufficientlylow so that sterilant solution 109 begins to boil and escapes throughannular path 120 as shown in FIG. 5.

Various combinations of the embodiments are possible. For example, achamber with two movable shelves could utilize three different containerapparatii on each shelf. A six pulse sterilization cycle could beproduced with only two movable shelves in this manner.

The invention could be used in chambers other than freeze dryers thathave movable shelves and are capable of being evacuated. Also, the orderin which the shelves move can vary. The top shelf could be stationaryand the lower shelves could move.

While the invention is susceptible to various modifications andalternative forms, the preferred embodiments have been described hereinin detail. It is to be understood, however, that it is not intended tolimit the invention to the specific forms disclosed. On the contrary, itis intended to cover all modifications and alternative forms fallingwithin the spirit and scope of the invention.

What is claimed is:
 1. A method for decontaminating a chamber system toa predetermined level, that comprises that steps of:a) providing achamber system having at least a lower and an upper half, at least oneof which is vertically movable while maintaining its horizontalposition, a condenser, and piping that are fluidly connected to eachother and to a vacuum system; b) placing at least one containercontaining a predetermined amount of liquid sterilant into the chamberon at least one shelf; c) placing a loose fitting cap on said at leastone container; d) moving one of the shelves until the adjacent shelfpresses against the at least one container cap thereby sealing thecontainer; e) evacuating the chamber, condenser and piping to a vacuumof below 1 Torr absolute pressure, wherein the chamber system isisolated from the vacuum system; f) moving another of said movableshelves until the cap on the at least one container is no longer sealedon the container; g) vaporizing at least a portion of said liquidsterilant by exposing said liquid sterilant to the evacuated chamberenvironment; and h) maintaining the vacuum and exposing the interior ofsaid chamber to sterilant vapor for a pre-determined time until apredetermined level of decontamination is achieved.
 2. The method ofclaim 1, wherein the liquid sterilant in said container is selected fromthe group consisting essentially of hydrogen peroxide and peracetic acidand mixtures thereof.
 3. The method of claim 1, wherein the liquidsterilant in said container is from between about 30% to about 35% byweight concentration of aqueous hydrogen peroxide solution.
 4. Themethod of claim 1, wherein the mass of liquid sterilant is smallcompared to the mass of the container to prevent freezing.
 5. The methodof claim 1, wherein the predetermined level of decontamination issterilization.
 6. The method of claim 1, wherein the chamber system is afreeze dryer system.
 7. The method of claim 1, wherein the methodfurther comprises repeating steps d) through h) for each additionalshelf until a predetermined level of decontamination is achieved.
 8. Amethod for decontaminating a chamber system that comprises the stepsof:a) providing a chamber system having a bottom, at least one middleand a top shelf, wherein at least two of the shelves are verticallymovable while maintaining a horizontal position and which can be stoppedin any position, a condenser, and piping that are fluidly connected toeach other and to a vacuum system; b) placing multiple containerscontaining a predetermined amount of liquid sterilant into the chamberon at least two of the shelves each of which is directly below andadjacent to one of the other shelves; c) placing a loose fitting cap oneach container; d) selectively moving each movable shelf to press thecaps and seal the containers on an adjacent shelf; e) evacuating thechamber, condenser and piping to a vacuum below 1 Torr absolutepressure, wherein the chamber system is isolated from the vacuum system;f) moving at least one of the movable shelves until the cap on eachcontainer on a respective adjacent shelf is released and the containeris no longer sealed; g) vaporizing the liquid sterilant in eachnon-sealed container by exposing the liquid to the evacuated chamber; h)maintaining the vacuum and exposing the interior of the chamber tosterilant vapor for a first pre-determined time; i) venting air into thechamber, thereby raising the pressure within the chamber to about atleast 50 Torr; j) evacuating the chamber, condenser and piping to avacuum of below 1 Torr absolute pressure, wherein the chamber system isisolated from the vacuum system; k) moving at least a second one of themovable shelves until the cap on each container on a respective adjacentshelf is released and the container is no longer sealed; l) vaporizingthe liquid sterilant in each non-sealed container by exposing the liquidto the evacuated chamber environment; and m) maintaining the vacuum andexposing the interior of said chamber to sterilant vapor for a secondpre-determined time until a predetermined level of decontamination isachieved.
 9. The method of claim 8, wherein the liquid sterilant isselected from the group consisting essentially of hydrogen peroxide andperacetic acid and mixtures thereof.
 10. The method of claim 8, whereinthe liquid sterilant is from between about 30% to about 35% by weightconcentration of aqueous hydrogen peroxide solution.
 11. The method ofclaim 8, wherein the predetermined amount of liquid hydrogen peroxide isdistributed among the containers placed on the chamber shelves.
 12. Themethod of claim 8, wherein the predetermined level of decontamination issterilization.
 13. The method of claim 8, wherein the chamber system isa freeze dryer system.
 14. A method for decontaminating a chambersystem, which comprises the steps of:a) providing a chamber systemhaving a plurality of shelves, at least one of which is verticallymovable while maintaining its horizontal position, a condenser, andpiping that are fluid connected to each other and to a vacuum system; b)placing n sets of containers, each set consisting of at least onecontainer, into the chamber on at least one of the shelves, eachcontainer containing a pre-determined amount of liquid sterilant, andwherein each container further comprises a cap assembly, a compressurespring, a plunger, a sealing device, and a bottom assembly such thateach set has a cap assembly of a different length; c) placing the capassembly loosely on each container; d) moving the movable shelves untilthe cap assembly on each container is pressed by one of the respectiveadjacent shelves and seals substantially all of the containers; e)evacuating the chamber, condenser and piping to a vacuum of below 1 Torrabsolute pressure, wherein the chamber system is isolated from thevacuum system; f) moving at least one of the movable shelves to a firstpredetermined level until the cap assembly is released and the seal onat least one set of the containers is broken; g) vaporizing the liquidsterilant by exposing said liquid to the evacuated chamber environment;h) maintaining the vacuum and exposing the interior of the chamber tosterilant vapor for a first pre-determined time; i) injecting air intothe chamber; j) re-evacuating the chamber, condenser and piping; k)moving at least another movable shelf to another predetermined leveluntil the cap assembly is released and the seal of at least oneadditional set of containers is broken; l) vaporizing the liquidsterilant by exposing said liquid to the evacuated chamber environment;m) maintaining the vacuum and exposing the interior of said chambersystem to sterilant vapor for another pre-determined time; and n)maintaining the vacuum and exposing the interior of the chamber systemto sterilant vapor until a predetermined level of decontamination isachieve.
 15. The method of claim 14, wherein the bottom assembly of saidcontainers has raised dimples permitting the area on the shelf below thecontainers to be sterilized.
 16. The method of claim 14, wherein theliquid sterilant is selected from the group consisting of hydrogenperoxide and peracetic acid and mixtures thereof.
 17. The method ofclaim 14, wherein the liquid hydrogen peroxide is from between about 30%to about 35% by weight concentration of aqueous hydrogen peroxidesolution.
 18. The method of claim 14, wherein the predetermined level ofdecontamination is sterilization.
 19. The method of claim 14, whereinthe chamber system is a freeze dryer system.
 20. The method of claim 14,wherein the liquid sterilant in each container is from about 1 to about2 grams of liquid hydrogen peroxide.
 21. The method of claim 14, whereinthe number of sets of containers, n, is any number between 2 and 20 andin which steps (e) through (g) are repeated once for each set ofcontainers.
 22. The method of claim 14, wherein the method furthercomprising repeating steps k) through m) until a predetermined level ofdecontamination is achieved.